Canonical Allele Identifier: CA351501629

Gene: RAF1

Linked Data

• MyVariant Identifiers: chr3:g.12632300A>G (hg19) ; chr3:g.12590801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12590801A>G , CM000665.2:g.12590801A>G	GRCh38
NC_000003.11:g.12632300A>G , CM000665.1:g.12632300A>G	GRCh37
NC_000003.10:g.12607300A>G	NCBI36
NG_007467.1:g.78379T>C , LRG_413:g.78379T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000423275.6:c.*1032T>C	ENSP00000401088.1:n.*1032T>C
ENST00000432427.3:c.684T>C
ENST00000460610.2:n.161T>C
ENST00000465826.6:n.958T>C
ENST00000475353.2:n.1289T>C
ENST00000494557.2:n.1178T>C
ENST00000684903.1:c.*1044T>C	ENSP00000508612.1:n.*1044T>C
ENST00000685348.1:c.*1044T>C	ENSP00000510285.1:n.*1044T>C
ENST00000685437.1:c.1268T>C	ENSP00000508794.1:p.Met423Thr
ENST00000685653.1:c.1367T>C	ENSP00000509968.1:p.Met456Thr
ENST00000685738.1:c.*331T>C	ENSP00000510156.1:n.*331T>C
ENST00000686409.1:n.2418T>C
ENST00000686455.1:n.1730T>C
ENST00000686762.1:c.1367T>C	ENSP00000509767.1:p.Met456Thr
ENST00000687257.1:n.1603T>C
ENST00000687326.1:c.*301T>C	ENSP00000509665.1:n.*301T>C
ENST00000687505.1:n.1485T>C
ENST00000687923.1:c.1256T>C	ENSP00000510255.1:p.Met419Thr
ENST00000687940.1:n.1744T>C
ENST00000688269.1:n.1963T>C
ENST00000688326.1:c.800T>C
ENST00000688444.1:n.1693T>C
ENST00000688543.1:c.1268T>C	ENSP00000509612.1:p.Met423Thr
ENST00000688625.1:c.*945T>C	ENSP00000509522.1:n.*945T>C
ENST00000688803.1:n.1598T>C
ENST00000688914.1:n.353T>C
ENST00000689097.1:c.*1044T>C	ENSP00000509756.1:n.*1044T>C
ENST00000689389.1:c.1193+907T>C	ENSP00000510213.1:n.1193+907T>C
ENST00000689418.1:c.*1044T>C	ENSP00000509467.1:n.*1044T>C
ENST00000689481.1:c.*1044T>C	ENSP00000510248.1:n.*1044T>C
ENST00000689540.1:n.1517T>C
ENST00000689876.1:c.1367T>C	ENSP00000508535.1:p.Met456Thr
ENST00000689914.1:c.*301T>C	ENSP00000509847.1:n.*301T>C
ENST00000690397.1:c.1256T>C	ENSP00000508730.1:p.Met419Thr
ENST00000690460.1:c.1355T>C	ENSP00000509106.1:p.Met452Thr
ENST00000690585.1:c.259T>C
ENST00000690625.1:n.2403T>C
ENST00000691396.1:c.*1219T>C	ENSP00000510712.1:n.*1219T>C
ENST00000691724.1:c.*324T>C	ENSP00000509255.1:n.*324T>C
ENST00000691779.1:c.*945T>C	ENSP00000508592.1:n.*945T>C
ENST00000691888.1:c.259T>C
ENST00000691899.1:c.1367T>C	ENSP00000508763.1:p.Met456Thr
ENST00000692069.1:n.1933T>C
ENST00000692093.1:c.1268T>C	ENSP00000509669.1:p.Met423Thr
ENST00000692311.1:n.2191T>C
ENST00000692558.1:n.1732T>C
ENST00000692773.1:c.*1104T>C	ENSP00000509055.1:n.*1104T>C
ENST00000692830.1:c.*1112T>C	ENSP00000509461.1:n.*1112T>C
ENST00000693069.1:c.*301T>C	ENSP00000510072.1:n.*301T>C
ENST00000693312.1:c.1142T>C	ENSP00000508686.1:p.Met381Thr
ENST00000693664.1:c.1367T>C	ENSP00000509614.1:p.Met456Thr
ENST00000693705.1:c.*1044T>C	ENSP00000510697.1:n.*1044T>C
ENST00000251849.9:c.1367T>C MANE Select	ENSP00000251849.4:p.Met456Thr
ENST00000442415.7:c.1427T>C	ENSP00000401888.2:p.Met476Thr
ENST00000251849.8:c.1367T>C	ENSP00000251849.4:p.Met456Thr
ENST00000423275.5:c.*1044T>C	ENSP00000401088.1:n.*1044T>C
ENST00000432427.2:c.1004T>C	ENSP00000398591.2:p.Met335Thr
ENST00000442415.6:c.1427T>C	ENSP00000401888.2:p.Met476Thr
ENST00000460610.1:n.324T>C
ENST00000465826.5:n.724T>C
ENST00000475353.1:n.535T>C
ENST00000494557.1:n.383T>C
NM_002880.3:c.1367T>C , LRG_413t1:c.1367T>C	NP_002871.1:p.Met456Thr
XM_005265355.1:c.1367T>C	XP_005265412.1:p.Met456Thr
XM_005265357.1:c.1268T>C	XP_005265414.1:p.Met423Thr
XM_005265358.3:c.1124T>C	XP_005265415.1:p.Met375Thr
XM_005265359.3:c.1025T>C	XP_005265416.1:p.Met342Thr
XM_005265360.1:c.1367T>C	XP_005265417.1:p.Met456Thr
XM_011533974.1:c.1367T>C	XP_011532276.1:p.Met456Thr
XM_011533975.1:c.1124T>C	XP_011532277.1:p.Met375Thr
NM_001354689.1:c.1427T>C	NP_001341618.1:p.Met476Thr
NM_001354690.1:c.1367T>C	NP_001341619.1:p.Met456Thr
NM_001354691.1:c.1124T>C	NP_001341620.1:p.Met375Thr
NM_001354692.1:c.1124T>C	NP_001341621.1:p.Met375Thr
NM_001354693.1:c.1268T>C	NP_001341622.1:p.Met423Thr
NM_001354694.1:c.1184T>C	NP_001341623.1:p.Met395Thr
NM_001354695.1:c.1025T>C	NP_001341624.1:p.Met342Thr
NR_148940.1:n.1895T>C
NR_148941.1:n.1841T>C
NR_148942.1:n.1780T>C
XM_011533974.3:c.1367T>C	XP_011532276.1:p.Met456Thr
XM_017006966.1:c.1268T>C	XP_016862455.1:p.Met423Thr
NM_001354689.3:c.1427T>C	NP_001341618.1:p.Met476Thr
NM_001354690.2:c.1367T>C	NP_001341619.1:p.Met456Thr
NM_001354691.2:c.1124T>C	NP_001341620.1:p.Met375Thr
NM_001354692.2:c.1124T>C	NP_001341621.1:p.Met375Thr
NM_001354693.2:c.1268T>C	NP_001341622.1:p.Met423Thr
NM_001354694.2:c.1184T>C	NP_001341623.1:p.Met395Thr
NM_001354695.2:c.1025T>C	NP_001341624.1:p.Met342Thr
NR_148940.2:n.1811T>C
NR_148941.2:n.1757T>C
NR_148942.2:n.1696T>C
NM_001354690.3:c.1367T>C	NP_001341619.1:p.Met456Thr
NM_001354691.3:c.1124T>C	NP_001341620.1:p.Met375Thr
NM_001354692.3:c.1124T>C	NP_001341621.1:p.Met375Thr
NM_001354693.3:c.1268T>C	NP_001341622.1:p.Met423Thr
NM_001354694.3:c.1184T>C	NP_001341623.1:p.Met395Thr
NM_001354695.3:c.1025T>C	NP_001341624.1:p.Met342Thr
NM_002880.4:c.1367T>C MANE Select	NP_002871.1:p.Met456Thr
NR_148940.3:n.1811T>C
NR_148941.3:n.1757T>C
NR_148942.3:n.1696T>C